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Characterization of arylalkylamine N-acetyltransferase from silkmoth (Antheraea pernyi) and pesticidal drug design based on the baculovirus-expressed enzyme
- Tsugehara, Taketo, Imai, Tetsuya, Takeda, Makio
- Comparative Biochemistry and Physiology, Part C 2013 v.157 pp. 93-102
- Antheraea pernyi, Bombyx mori, amino acid sequences, amino acids, biochemical pathways, complementary DNA, dopamine, insecticides, insects, norepinephrine, octopamine, physiology, polymerase chain reaction, screening, sequence analysis, serotonin, tryptamine, tyramine, vertebrates
- Arylalkylamine N-acetyltransferase (AANAT; EC 22.214.171.124) catalyzes the N-acetylation of arylalkylamines. A cDNA encoding AANAT (ApAANAT) was cloned from Antheraea pernyi by PCR. The cDNA of 1966bp encodes a 261 amino acid protein. The amino acid sequence was found to have a high homology with Bombyx mori AANAT (BmNAT) but had very low homology with vertebrate AANATs. Amino acid sequence analysis revealed that four insect AANATs cloned from three species including ApAANAT formed a distinct cluster from the vertebrate group. A recombinant ApAANAT protein was expressed in Sf9 cells using a baculovirus expression system, having AANAT activity. The transformed cell extract acetylated tryptamine, serotonin, dopamine, tyramine, octopamine and norepinephrine. The AANAT activity was inhibited at over 0.03mM tryptamine. Although insect AANATs have been considered as a target of insecticide, this type of insecticide has never been developed. Screening a chemical library of Otsuka Chemical Co., Ltd., we found a novel compound and its derivatives that inhibited the AANAT activity of ApAANAT. This may facilitate investigation of the monoamine metabolic pathway in insects and the development of new types of insecticides and inhibitors of AANATs.